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肢体及特定任务性肌张力障碍的研究重点

Research Priorities in Limb and Task-Specific Dystonias.

作者信息

Pirio Richardson Sarah, Altenmüller Eckart, Alter Katharine, Alterman Ron L, Chen Robert, Frucht Steven, Furuya Shinichi, Jankovic Joseph, Jinnah H A, Kimberley Teresa J, Lungu Codrin, Perlmutter Joel S, Prudente Cecília N, Hallett Mark

机构信息

Department of Neurology, University of New Mexico Health Sciences Center, Albuquerque, NM, USA.

Institute for Music Physiology and Musicians' Medicine (IMMM), Hannover University of Music, Drama and Media, Hannover, Germany.

出版信息

Front Neurol. 2017 May 3;8:170. doi: 10.3389/fneur.2017.00170. eCollection 2017.

Abstract

Dystonia, which causes intermittent or sustained abnormal postures and movements, can present in a focal or a generalized manner. In the limbs, focal dystonia can occur in either the upper or lower limbs and may be task-specific causing abnormal motor performance for only a specific task, such as in writer's cramp, runner's dystonia, or musician's dystonia. Focal limb dystonia can be non-task-specific and may, in some circumstances, be associated with parkinsonian disorders. The true prevalence of focal limb dystonia is not known and is likely currently underestimated, leaving a knowledge gap and an opportunity for future research. The pathophysiology of focal limb dystonia shares some commonalities with other dystonias with a loss of inhibition in the central nervous system and a loss of the normal regulation of plasticity, called homeostatic plasticity. Functional imaging studies revealed abnormalities in several anatomical networks that involve the cortex, basal ganglia, and cerebellum. Further studies should focus on distinguishing cause from effect in both physiology and imaging studies to permit focus on most relevant biological correlates of dystonia. There is no specific therapy for the treatment of limb dystonia given the variability in presentation, but off-label botulinum toxin therapy is often applied to focal limb and task-specific dystonia. Various rehabilitation techniques have been applied and rehabilitation interventions may improve outcomes, but small sample size and lack of direct comparisons between methods to evaluate comparative efficacy limit conclusions. Finally, non-invasive and invasive therapeutic modalities have been explored in small studies with design limitations that do not yet clearly provide direction for larger clinical trials that could support new clinical therapies. Given these gaps in our clinical, pathophysiologic, and therapeutic knowledge, we have identified priorities for future research including: the development of diagnostic criteria for limb dystonia, more precise phenotypic characterization and innovative clinical trial design that considers clinical heterogeneity, and limited available number of participants.

摘要

肌张力障碍会导致间歇性或持续性异常姿势和动作,可呈局灶性或全身性表现。在肢体方面,局灶性肌张力障碍可发生在上肢或下肢,且可能与特定任务相关,仅在特定任务时导致异常运动表现,如书写痉挛、跑步者肌张力障碍或音乐家肌张力障碍。局灶性肢体肌张力障碍也可能与特定任务无关,在某些情况下,可能与帕金森病相关。局灶性肢体肌张力障碍的真实患病率尚不清楚,目前可能被低估,这留下了知识空白以及未来研究的机会。局灶性肢体肌张力障碍的病理生理学与其他肌张力障碍有一些共同之处,即中枢神经系统抑制功能丧失以及正常的可塑性调节(称为稳态可塑性)丧失。功能影像学研究揭示了涉及皮层、基底神经节和小脑的多个解剖学网络存在异常。进一步的研究应专注于在生理学和影像学研究中区分因果关系,以便聚焦于肌张力障碍最相关的生物学关联因素。鉴于临床表现的变异性,目前尚无治疗肢体肌张力障碍的特异性疗法,但肉毒杆菌毒素的非适应证治疗常应用于局灶性肢体和特定任务相关的肌张力障碍。已应用了各种康复技术,康复干预可能改善预后,但样本量小以及缺乏方法之间的直接比较以评估相对疗效限制了结论。最后,在一些设计存在局限性的小型研究中探索了非侵入性和侵入性治疗方式,这些研究尚未明确为可支持新临床疗法的大型临床试验提供方向。鉴于我们在临床、病理生理和治疗知识方面存在这些差距,我们确定了未来研究的重点,包括:制定肢体肌张力障碍的诊断标准、更精确的表型特征描述以及考虑临床异质性和参与者数量有限的创新型临床试验设计。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fd2/5413505/4152036c3e63/fneur-08-00170-g001.jpg

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